Patient-Specific Instrumentation Does Not Improve Alignment Compared to the Extramedullary Foot Holder for the INBONE II Total Ankle Arthroplasty.

IF 2.2
Charlotte H Jones, Allison Boden, Patricia Friedmann, Suzy Wang, Ricardo Villar, Constantine Demetracopoulos, Jonathan Deland, Elizabeth Cody, Matthew S Conti, Jensen K Henry, Scott J Ellis
{"title":"Patient-Specific Instrumentation Does Not Improve Alignment Compared to the Extramedullary Foot Holder for the INBONE II Total Ankle Arthroplasty.","authors":"Charlotte H Jones, Allison Boden, Patricia Friedmann, Suzy Wang, Ricardo Villar, Constantine Demetracopoulos, Jonathan Deland, Elizabeth Cody, Matthew S Conti, Jensen K Henry, Scott J Ellis","doi":"10.1177/10711007251353787","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Patient-specific instrumentation (PSI) was developed to improve accuracy and efficiency in implant placement for total ankle arthroplasty (TAA). This study represents the first to measure the accuracy of PSI regarding implant alignment and implant size in the INBONE II total ankle system (Stryker). A secondary goal was to compare radiographic and clinical outcomes between the PSI and that of a matched group of implants performed with standard instrumentation.</p><p><strong>Methods: </strong>This retrospective study of 92 patients (46 PSI and 46 non-PSI cases matched by age and sex) was performed at a single institution between 2006 and 2024, including TAA patients with INBONE II implants. Median age was 61 years (range 27-81). Median body mass index (BMI) was 29.6 (range 19.9-45.6). One surgeon performed 71% of PSI. A different surgeon performed 96% of non-PSI cases. PSI alignment (tibiotalar angle [TTA]), deformity correction (talar-tilt [TT]), radiation exposure, tourniquet, and operative time were compared to the standard jig method (non-PSI). Total fluoroscopy, tourniquet and procedure time, and preoperative and postoperative radiographs were analyzed.</p><p><strong>Results: </strong>PSI predicted the correct size in 67% (n = 31) of talus implants and 89% (n = 41) of tibial implants. Median absolute deviation in the mortise view was 1.3 (IQR 0.53-2.18) and 1.8 (IQR 1.35-3.5) in the lateral view. For both groups, postoperative median TTA deviation was less than 2 degrees and postoperative median TT was less than or equal to 1 degree. Median fluoroscopic time was 92.1 seconds for PSI and 104.3 seconds for non-PSI. PSI had a longer tourniquet (156.5 vs 134.5 minutes) and procedure time (188 vs 161 minutes) compared with non-PSI.</p><p><strong>Conclusion: </strong>In this study of stemmed TAA implants, surgeons achieved alignment generally consistent with PSI predictions. PSI adequately predicted implant size. For most cases, PSI achieved similar alignment and correction of deformity compared with standard instrumentation. PSI did not improve radiographic alignment compared with traditional instrumentation and was associated with longer operative times, possibly reflecting the primary surgeon's early experience with the technique. Each surgeon should select PSI or the standard jig based on their experience and preference.</p>","PeriodicalId":94011,"journal":{"name":"Foot & ankle international","volume":" ","pages":"10711007251353787"},"PeriodicalIF":2.2000,"publicationDate":"2025-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Foot & ankle international","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/10711007251353787","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Patient-specific instrumentation (PSI) was developed to improve accuracy and efficiency in implant placement for total ankle arthroplasty (TAA). This study represents the first to measure the accuracy of PSI regarding implant alignment and implant size in the INBONE II total ankle system (Stryker). A secondary goal was to compare radiographic and clinical outcomes between the PSI and that of a matched group of implants performed with standard instrumentation.

Methods: This retrospective study of 92 patients (46 PSI and 46 non-PSI cases matched by age and sex) was performed at a single institution between 2006 and 2024, including TAA patients with INBONE II implants. Median age was 61 years (range 27-81). Median body mass index (BMI) was 29.6 (range 19.9-45.6). One surgeon performed 71% of PSI. A different surgeon performed 96% of non-PSI cases. PSI alignment (tibiotalar angle [TTA]), deformity correction (talar-tilt [TT]), radiation exposure, tourniquet, and operative time were compared to the standard jig method (non-PSI). Total fluoroscopy, tourniquet and procedure time, and preoperative and postoperative radiographs were analyzed.

Results: PSI predicted the correct size in 67% (n = 31) of talus implants and 89% (n = 41) of tibial implants. Median absolute deviation in the mortise view was 1.3 (IQR 0.53-2.18) and 1.8 (IQR 1.35-3.5) in the lateral view. For both groups, postoperative median TTA deviation was less than 2 degrees and postoperative median TT was less than or equal to 1 degree. Median fluoroscopic time was 92.1 seconds for PSI and 104.3 seconds for non-PSI. PSI had a longer tourniquet (156.5 vs 134.5 minutes) and procedure time (188 vs 161 minutes) compared with non-PSI.

Conclusion: In this study of stemmed TAA implants, surgeons achieved alignment generally consistent with PSI predictions. PSI adequately predicted implant size. For most cases, PSI achieved similar alignment and correction of deformity compared with standard instrumentation. PSI did not improve radiographic alignment compared with traditional instrumentation and was associated with longer operative times, possibly reflecting the primary surgeon's early experience with the technique. Each surgeon should select PSI or the standard jig based on their experience and preference.

INBONE II全踝关节置换术中,与髓外足架相比,患者专用内固定不能改善对齐。
背景:患者特异性内固定(PSI)的发展是为了提高全踝关节置换术(TAA)植入物的准确性和效率。该研究首次测量了在INBONE II全踝系统中PSI对植入物对准和植入物大小的准确性(Stryker)。第二个目的是比较PSI和使用标准器械植入的匹配组的放射学和临床结果。方法:本研究回顾性研究了2006年至2024年间在一家机构进行的92例患者(46例PSI和46例年龄和性别匹配的非PSI),包括使用INBONE II植入物的TAA患者。中位年龄61岁(范围27-81岁)。中位体重指数(BMI)为29.6(范围19.9-45.6)。一名外科医生执行了71%的PSI。另一位外科医生处理了96%的非psi病例。将PSI对准(胫距角[TTA])、畸形矫正(距距倾斜[TT])、辐射暴露、止血带和手术时间与标准夹具法(非PSI)进行比较。分析全透视、止血带和手术时间,以及术前和术后x线片。结果:PSI预测距骨假体尺寸的正确率为67% (n = 31),胫骨假体的正确率为89% (n = 41)。槽位位绝对偏差中位数为1.3 (IQR 0.53-2.18),侧位位绝对偏差中位数为1.8 (IQR 1.35-3.5)。两组术后中位TTA偏差均小于2度,中位TT均小于或等于1度。PSI组透视时间中位数为92.1秒,非PSI组为104.3秒。与非PSI相比,PSI的止血带时间更长(156.5分钟对134.5分钟),手术时间更长(188分钟对161分钟)。结论:在本研究中,外科医生实现了与PSI预测基本一致的对齐。PSI可以充分预测种植体的大小。在大多数情况下,与标准内固定相比,PSI实现了相似的对准和畸形矫正。与传统器械相比,PSI并没有改善影像学对准,而且与更长的手术时间有关,这可能反映了初级外科医生对该技术的早期经验。每位外科医生应根据自己的经验和喜好选择PSI或标准夹具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信